Arriola Edurne, González-Cao María, Domine Manuel, De Castro Javier, Cobo Manuel, Bernabé Reyes, Navarro Alejandro, Sullivan Ivana, Trigo José Manuel, Mosquera Joaquín, Crama Leonardo, Isla Dolores
Medical Oncology Department, Hospital Universitari del Mar-CIBERONC, Passeig Marítim 25-29, 08003, Barcelona, Spain.
Medical Oncology Department (IOR), Hospital Dexeus, Barcelona, Spain.
Oncol Ther. 2022 Jun;10(1):167-184. doi: 10.1007/s40487-021-00182-0. Epub 2022 Jan 15.
The addition of immune checkpoint inhibitors (ICIs) to conventional chemotherapy (CT) as first-line treatment improves survival in extensive-stage small-cell lung cancer (ES-SCLC). The aim of this meta-analysis was to determine the relative efficacy of first-line ICIs compared with CT in patients with ES-SCLC.
Two independent reviewers extracted relevant data according to PRISMA guidelines and assessed the risk of bias using the Cochrane Collaboration's risk-of-bias tool. Meta-analysis was conducted using random-effects models to calculate an average effect size for overall survival (OS), progression-free survival (PFS), and safety outcomes in the overall populations and clinically relevant subgroups.
A literature search of PubMed and Embase was performed. Six randomized controlled clinical trials (IMpower133, CHECKMATE-451, CASPIAN, KEYNOTE-604, and phase II and III ipilimumab plus CT trials) with a total of 3757 patients were included. Compared with CT alone, ICIs plus CT showed a favourable effect on OS (hazard ratio [HR] 0.85; 95% confidence intervals [CI] 0.79-0.96) and PFS (HR 0.78; 95% CI 0.72-0.83) but a non-significant increase in the risk of experiencing any adverse event (relative risk, 1.05; 95% CI 0.99-1.11). The estimated HR for OS favoured ICI combinations in all planned subgroups according to age (< 65 years/≥ 65 years), sex (men/women), and ECOG performance status (0/1). Analysis by specific ICI revealed significant improvements in OS only for atezolizumab + CT (HR 1.36; 95% CI 1.09-1.69) and durvalumab + CT (HR 1.35; 95% CI 1.12-1.62) compared with CT alone.
Combining anti-programmed cell death ligand 1 antibodies with platinum/etoposide is a superior therapeutic approach compared to CT alone for the first-line treatment of patients with ES-SCLC.
在广泛期小细胞肺癌(ES-SCLC)的一线治疗中,将免疫检查点抑制剂(ICI)添加到传统化疗(CT)中可提高生存率。本荟萃分析的目的是确定一线ICI与CT相比在ES-SCLC患者中的相对疗效。
两名独立审阅者根据PRISMA指南提取相关数据,并使用Cochrane协作网的偏倚风险工具评估偏倚风险。采用随机效应模型进行荟萃分析,以计算总体人群和临床相关亚组的总生存期(OS)、无进展生存期(PFS)和安全性结局的平均效应量。
对PubMed和Embase进行了文献检索。纳入了六项随机对照临床试验(IMpower133、CHECKMATE-451、CASPIAN、KEYNOTE-604以及II期和III期伊匹木单抗联合CT试验),共3757例患者。与单纯CT相比,ICI联合CT对OS(风险比[HR]0.85;95%置信区间[CI]0.79-0.96)和PFS(HR 0.78;95%CI 0.72-0.83)显示出有利影响,但发生任何不良事件的风险无显著增加(相对风险,1.05;95%CI 0.99-1.11)。根据年龄(<65岁/≥65岁)、性别(男性/女性)和东部肿瘤协作组(ECOG)体能状态(0/1),在所有计划亚组中,OS的估计HR均有利于ICI联合治疗。按特定ICI进行分析显示,与单纯CT相比,仅阿替利珠单抗联合CT(HR 1.36;95%CI 1.09-1.69)和度伐利尤单抗联合CT(HR 1.35;95%CI 1.12-1.62)的OS有显著改善。
与单纯CT相比,将抗程序性细胞死亡配体1抗体与铂类/依托泊苷联合使用是ES-SCLC患者一线治疗的更优治疗方法。